EP0150026A3 - Chemisches Verfahren - Google Patents
Chemisches Verfahren Download PDFInfo
- Publication number
- EP0150026A3 EP0150026A3 EP85100279A EP85100279A EP0150026A3 EP 0150026 A3 EP0150026 A3 EP 0150026A3 EP 85100279 A EP85100279 A EP 85100279A EP 85100279 A EP85100279 A EP 85100279A EP 0150026 A3 EP0150026 A3 EP 0150026A3
- Authority
- EP
- European Patent Office
- Prior art keywords
- optionally
- compound
- halogen
- oxidation
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000001311 chemical methods and process Methods 0.000 title abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 230000002378 acidificating effect Effects 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 230000003647 oxidation Effects 0.000 abstract 3
- 238000007254 oxidation reaction Methods 0.000 abstract 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 229910052740 iodine Inorganic materials 0.000 abstract 2
- 239000011630 iodine Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000003363 1,3,5-triazinyl group Chemical group N1=C(N=CN=C1)* 0.000 abstract 1
- -1 1,4-diazinyl Chemical group 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000005956 isoquinolyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 125000005493 quinolyl group Chemical group 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- 150000003464 sulfur compounds Chemical class 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C07D235/32—Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B45/00—Formation or introduction of functional groups containing sulfur
- C07B45/06—Formation or introduction of functional groups containing sulfur of mercapto or sulfide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/22—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides
- C07C319/24—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides by reactions involving the formation of sulfur-to-sulfur bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
- C07C321/12—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms
- C07C321/14—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
- C07C321/24—Thiols, sulfides, hydropolysulfides, or polysulfides having thio groups bound to carbon atoms of six-membered aromatic rings
- C07C321/28—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/65—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
R - X - R¹ (I),
(X = -S-, -S-S-, -CO-,
R und R¹ = unabhängig voneinander H, OH;
gegebenenfalls durch mindestens ein OH, Carboxy, C₁₋₆- Alkoxycarbonyl, NH₂, Acetylamino, NO₂, C₁₋₆-Alkylamino, C₁₋₆-Alkoxy, gegebenenfalls durch mindestens ein OH subst, C₅₋₇- Cycloalkyl und/oder durch Halogen subst. C₁₋₁₂-Alkyl oder C₂₋₁₂-Alkenyl; C₇₋₁₀-Aralkyl; gegebenenfalls durch minde stens ein C₁₋₄-Alkyl, NO₂ und/oder Halogen subst. Phenyl oder Naphthyl; 5- oder 6-gliedriger, 1-3 Stickstoffatome enthaltender, gegebenenfalls mit einem Benzolring konden sierter und gegebenenfalls mindestens einen Substituenten enthaltenden Heterocyclus - vorzugsweise 2-Carbometho xyamino-1H-benzimidazol-5-yl, Pyrrolyl, Indolyl, Imidazolyl, Benzimidazolyl, Pyridyl, Chinolyl, Isochinolyl, 1,2-, 1,3- oder 1,4-Diazinyl, 1,2,4- oder 1,3,5-Triazinyl, Phthalazinyl oder Chinoxalyl; halogensubst. C₁₋₁₀-Aralkyl oder
-(CH₂)n-Halogen (n = 1 - 6))
durch Reduktion einer Verbindung der Formel II
R-A (II)
(A = Chlorfulfonyl, --R¹
oder --R¹,
R und R¹ wie oben)
mit einer Schwefelverbindung, die ein S-Atom mit dem Oxydationsgrad (+)4 enthält, der während der Reaktion in den Oxydationsgrad (+)6 überführbar ist oder in saurem Medium zu einer Verbindung mit dem letztgenannten Oxy dationsgrad zersetzt werden kann, in Gegenwart von höch stens 0,5 Mol / 1 Mol Ausgangsverbindung der Formel I, vorzugsweise einer katalytischen Menge, elementarem Jod oder einer Verbindung, die in saurem Medium Jodwasser stoff liefert, oder in saurem Medium mit der verwendeten
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU84154A HU192973B (en) | 1984-01-16 | 1984-01-16 | New process for reducing sulfochlorides, sulfoxides and alpha-halogenocarbonyl compounds for producing dithio-, thio- or carbonyl compounds |
| HU15484 | 1984-11-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0150026A2 EP0150026A2 (de) | 1985-07-31 |
| EP0150026A3 true EP0150026A3 (de) | 1986-02-12 |
Family
ID=10948211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP85100279A Withdrawn EP0150026A3 (de) | 1984-01-16 | 1985-01-12 | Chemisches Verfahren |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4656290A (de) |
| EP (1) | EP0150026A3 (de) |
| JP (1) | JPS6133131A (de) |
| HU (1) | HU192973B (de) |
| SU (1) | SU1551244A3 (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3633968A1 (de) * | 1986-10-06 | 1988-04-07 | Hoechst Ag | Chirale aryl-2,3-epoxyalkyl-ether und deren entsprechende thioverbindungen und ihre verwendung als dotierstoff in fluessigkristall-phasen |
| FR2647117A1 (de) * | 1989-05-18 | 1990-11-23 | Elf France | |
| KR100654208B1 (ko) * | 2005-12-05 | 2006-12-06 | 주식회사 제이엠씨 | 방향족 디설파이드의 제조방법 |
| JP5482233B2 (ja) * | 2010-01-27 | 2014-05-07 | 宇部興産株式会社 | ジアリールジスルフィド化合物の製造方法 |
| JP6269300B2 (ja) * | 2014-05-01 | 2018-01-31 | 国立大学法人大阪大学 | スルホキシドの脱酸素用触媒、及び該脱酸素用触媒を用いたスルフィドの製造方法 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4069259A (en) * | 1976-10-19 | 1978-01-17 | Allied Chemical Corporation | Process for preparing organic disulfides |
| EP0093363A1 (de) * | 1982-04-30 | 1983-11-09 | CASSELLA Aktiengesellschaft | Verfahren zur Herstellung von Disulfiden |
-
1984
- 1984-01-16 HU HU84154A patent/HU192973B/hu not_active IP Right Cessation
-
1985
- 1985-01-12 EP EP85100279A patent/EP0150026A3/de not_active Withdrawn
- 1985-01-14 JP JP344185A patent/JPS6133131A/ja active Pending
- 1985-01-15 SU SU853845845A patent/SU1551244A3/ru active
- 1985-01-16 US US06/691,972 patent/US4656290A/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4069259A (en) * | 1976-10-19 | 1978-01-17 | Allied Chemical Corporation | Process for preparing organic disulfides |
| EP0093363A1 (de) * | 1982-04-30 | 1983-11-09 | CASSELLA Aktiengesellschaft | Verfahren zur Herstellung von Disulfiden |
Non-Patent Citations (2)
| Title |
|---|
| SYNTHESIS, Communications, Juli 1978, Seite 542, Georg Thieme Publishers. J. DRABOWICZ et al.: "An iodine-catalysed reduction of sulphoxides by formamidinesulphinic acid." * |
| THE JOURNAL OF ORGANIC CHEMISTRY; Band 34, Nr.8, August 1969, pages 2336-2339; Easton, US G.A. RUSSELL et al.: "Beta-keto sulfoxides. IV. Conversion into beta-keto sulfides, vinyl ethers, and enol acetates." * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0150026A2 (de) | 1985-07-31 |
| HUT40404A (en) | 1986-12-28 |
| HU192973B (en) | 1987-08-28 |
| SU1551244A3 (ru) | 1990-03-15 |
| JPS6133131A (ja) | 1986-02-17 |
| US4656290A (en) | 1987-04-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Designated state(s): AT CH DE FR GB IT LI |
|
| RHK1 | Main classification (correction) |
Ipc: C07B 45/06 |
|
| PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
| AK | Designated contracting states |
Designated state(s): AT CH DE FR GB IT LI |
|
| RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT. |
|
| 17P | Request for examination filed |
Effective date: 19860408 |
|
| RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT. |
|
| 17Q | First examination report despatched |
Effective date: 19870814 |
|
| RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT. |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 19910507 |
|
| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: KALDOR, ISTVAN, DIPL. ING. CHEM. Inventor name: HEIZER, JOZSEF, DIPL. ING. CHEM. Inventor name: BENEDEK, GEB. HARASZIN, EVA Inventor name: SZASZ, ANDRAS, DIPL. ING. CHEM. Inventor name: VEGH, GEB. BAJI, ILONA |